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银屑病的新药与治疗靶点

New drugs and treatment targets in psoriasis.

作者信息

Kofoed Kristian, Skov Lone, Zachariae Claus

机构信息

Department of Dermatovenereology, Copenhagen University Hospital, Bispebjerg, DK-2400 Copenhagen, Denmark.

出版信息

Acta Derm Venereol. 2015 Feb;95(2):133-9. doi: 10.2340/00015555-1931.

Abstract

In recent years, the increased understanding of the pathophysiology of psoriasis has resulted in several new treatments. The success of ustekinumab proved the importance of the IL-23/T helper cell 17 axis in psoriatic diseases. Several new biologics targeting this axis will reach the clinic in the next years. Biologics are costly, require injections, and some patients experience tacaphylaxis, thus, the development of orally available, small-molecule inhibitors is desirable. Among small-molecules under investigation are A3 adenosine receptor agonists, Janus kinase inhibitors, and phosphodiesterase inhibitors. We review published clinical trials, and conference abstracts presented during the last years, concerned with new drugs under development for the treatment of psoriasis. In conclusion, our psoriasis armamentarium will be filled with several new effective therapeutic options the coming years. We need to be aware of the limitations of drug safety data when selecting new novel treatments. Monitoring and clinical registries are still important tools.

摘要

近年来,对银屑病病理生理学认识的加深带来了几种新的治疗方法。优特克单抗的成功证明了白细胞介素-23/辅助性T细胞17轴在银屑病相关疾病中的重要性。未来几年,几种针对该轴的新型生物制剂将进入临床应用。生物制剂成本高昂,需要注射给药,且一些患者会出现过敏反应,因此,开发口服可用的小分子抑制剂是很有必要的。正在研究的小分子药物包括A3腺苷受体激动剂、Janus激酶抑制剂和磷酸二酯酶抑制剂。我们回顾了过去几年发表的有关正在研发的用于治疗银屑病的新药的临床试验及会议摘要。总之,未来几年我们治疗银屑病的手段将会有几种新的有效治疗选择。在选择新的治疗方法时,我们需要意识到药物安全性数据的局限性。监测和临床登记仍然是重要的工具。

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